Specimens were analyzed in a Bio-Rad Radiance Plus confocal scanning microscope (Bio-Rad, Hemel, Hempstead, UK) installed on a Nikon Eclipse E 600 fluorescence microscope (Nikon, Tokyo, Japan) and, in some experiments, an LSM 700 confocal microscope (Zeiss, Oberkochen, Germany) as in previous work [122 (link)]. The percentage of +NPs in DRGs was obtained as described [115 (link)]. Four to 8 sections of each DRG from 5 animals in each group were included in the analysis. The size distribution of +NPs with a visible nucleus was measured using the Nikon Eclipse E 600 fluorescence microscope with Wasabi Image Software. The +NPs were divided into small, medium-sized and large according to earlier studies [53 (link)]. The relative fluorescence levels (intensity) of sst2A-like immunoreactivity (LI) in DRGs before and after nerve injury were measured as described [115 (link)] using a Sarastro 1000 confocal laser-scanning system (Molecular Dynamics, Sunnyvale, Calif., USA).
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